Human Genome Epidemiology Literature Finder
Records 1 - 23 (of 23 Records) |
Query Trace: SCNN1A[original query] |
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Association of a sodium channel alpha subunit promoter variant with blood pressure. Journal of the American Society of Nephrology : JASN 2002 Jan 13 (1): 80-5. Iwai Naoharu, Baba Shunroku, Mannami Toshifumi, Ogihara Toshio, Ogata J |
The TNFalpha receptor TNFRSF1A and genes encoding the amiloride-sensitive sodium channel ENaC as modulators in cystic fibrosis. Human genetics 2006 Apr 119 (3): 331-43. Stanke Frauke, Becker Tim, Cuppens Harry, Kumar Vinod, Cassiman Jean-Jacques, Jansen Silke, Radojkovic Dragica, Siebert Benny, Yarden Jennifer, Ussery David W, Wienker Thomas F, Tümmler Burkha |
Genetic variation in the renal sodium transporters NKCC2, NCC, and ENaC in relation to the effects of loop diuretic drugs. Clinical pharmacology and therapeutics 2007 Sep 82 (3): 300-9. Vormfelde S V, Sehrt D, Toliat M R, Schirmer M, Meineke I, Tzvetkov M, Nürnberg P, Brockmöller |
Genetic analysis of Rwandan patients with cystic fibrosis-like symptoms: identification of novel cystic fibrosis transmembrane conductance regulator and epithelial sodium channel gene variants. Chest 2009 May 135 (5): 1233-42. Mutesa Léon, Azad Abul Kalam, Verhaeghe Catherine, Segers Karin, Vanbellinghen Jean-François, Ngendahayo Louis, Rusingiza Emmanuel Kamanzi, Mutwa Philippe Rutwaza, Rulisa Stephen, Koulischer Lucien, Cassiman Jean-Jacques, Cuppens Harry, Bours Vince |
Pharmacogenetic association of hypertension candidate genes with fasting glucose in the GenHAT Study. Journal of hypertension 2010 Oct 28 (10): 2076-83. Irvin Marguerite R, Lynch Amy I, Kabagambe Edmond K, Tiwari Hemant K, Barzilay Joshua I, Eckfeldt John H, Boerwinkle Eric, Davis Barry R, Ford Charles E, Arnett Donna |
Genetic variations in the sodium balance-regulating genes ENaC, NEDD4L, NDFIP2 and USP2 influence blood pressure and hypertension. Kidney & blood pressure research 2010 1 33 (1): 15-23. Jin Hyun-Seok, Hong Kyung-Won, Lim Ji-Eun, Hwang Sue-Yun, Lee Sang-Ho, Shin Chol, Park Hun Kuk, Oh Bermse |
Genetic variation of aENaC influences lung diffusion during exercise in humans. Respiratory physiology & neurobiology 2011 Dec 179 (2-3): 212-8. Baker Sarah E, Wheatley Courtney M, Cassuto Nicholas A, Foxx-Lupo William T, Sprissler Ryan, Snyder Eric |
Common variants in epithelial sodium channel genes contribute to salt sensitivity of blood pressure: The GenSalt study. Circulation. Cardiovascular genetics 2011 Aug 4 (4): 375-80. Zhao Qi, Gu Dongfeng, Hixson James E, Liu De-Pei, Rao Dabeeru C, Jaquish Cashell E, Kelly Tanika N, Lu Fanghong, Ma Jixiang, Mu Jianjun, Shimmin Lawrence C, Chen Jichun, Mei Hao, Hamm L Lee, He Jiang, |
Genetic variation of SCNN1A influences lung diffusing capacity in cystic fibrosis. Medicine and science in sports and exercise 2012 Dec 44 (12): 2315-21. Baker Sarah E, Wong Eric C, Wheatley Courtney M, Foxx-Lupo William T, Martinez Marina G, Morgan Mary A, Sprissler Ryan, Morgan Wayne J, Snyder Eric |
Genetic variation in putative salt taste receptors and salt taste perception in humans. Chemical senses 2013 Feb 38 (2): 137-45. Dias Andre G, Rousseau Dérick, Duizer Lisa, Cockburn Moira, Chiu Winnie, Nielsen Daiva, El-Sohemy Ahm |
Effects of rare and common blood pressure gene variants on essential hypertension: results from the Family Blood Pressure Program, CLUE, and Atherosclerosis Risk in Communities studies. Circulation research 2012 Nov . Nguyen KD, Pihur V, Ganesh SK, Rakha A, Cooper RS, Hunt SC, Freeman BI, Coresh J, Kao LW, Morrison AC, Boerwinkle E, Ehret GB, Chakravarti A |
Evidence of genetic association between TNFRSF1A encoding the p55 tumour necrosis factor receptor, and ankylosing spondylitis in UK Caucasians. Clinical and experimental rheumatology 0 30 (1): 110-3. Karaderi T, Pointon J J, Wordsworth T W H, Harvey D, Appleton L H, Cohen C J, Farrar C, Harin A, Brown M A, Wordsworth B P, |
Considering the vascular hypothesis for the pathogenesis of small intestinal atresia: a case control study of genetic factors. American journal of medical genetics. Part A 2013 Apr 161A (4): 702-10. Gupta Tanya, Yang Wei, Iovannisci David M, Carmichael Suzan L, Stevenson David K, Shaw Gary M, Lammer Edward |
Associations of epithelial sodium channel genes with blood pressure: the GenSalt study. Journal of human hypertension 2015 Apr 29 (4): 224-8. Liu F, Yang X, Mo X, Huang J, Chen J, Kelly T N, Hixson J E, Rao D C, Gu C C, Shimmin L C, Chen J, Rice T K, Li J, Schwander K, He J, Liu D-P, Gu |
Association analysis of four candidate genetic variants with sporadic amyotrophic lateral sclerosis in a Chinese population. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2014 Jul 35 (7): 1089-95. Chen Xueping, Huang Rui, Chen Yongping, Zheng Zhenzhen, Chen Ke, Song Wei, Zhao Bi, Yang Yuan, Yuan Lixing, Shang Huifa |
Assessment of epithelial sodium channel variants in nonwhite cystic fibrosis patients with non-diagnostic CFTR genotypes. Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society 2015 Apr . Brennan Marie-Luise, Pique Lynn M, Schrijver Ir |
Pharmacogenetic Effects of Inhaled Salbutamol on 10-km Time Trial Performance in Competitive Male and Female Cyclists. Clinical journal of sport medicine : official journal of the Canadian Academy of Sport Medicine 2015 Apr . Koch Sarah, MacInnis Martin J, Rupert James L, Sporer Benjamin C, Koehle Michael |
Resequencing Epithelial Sodium Channel Genes Identifies Rare Variants Associated With Blood Pressure Salt-Sensitivity: The GenSalt Study. American journal of hypertension 2017 10 31 (2): 205-211. Gu Xiaoying, Gu Dongfeng, He Jiang, Rao Dabeeru C, Hixson James E, Chen Jichun, Li Jianxin, Huang Jianfeng, Wu Xigui, Rice Treva K, Shimmin Lawrence C, Kelly Tanika |
Association of Genetic Variation in the Epithelial Sodium Channel Gene with Urinary Sodium Excretion and Blood Pressure. Nutrients 2018 May 10 (5): . Yang Yoon Jung, Kim Jihye, Kwock Chang Ke |
Premature Stroke Secondary to Severe Hypertension Results from Liddle Syndrome Caused by a Novel SCNN1B Mutation. Kidney & blood pressure research 2020 7 45 (4): 603-611. Fan Peng, Zhang Di, Pan Xiao-Cheng, Yang Kun-Qi, Zhang Qiong-Yu, Lu Yi-Ting, Zhang Ying, Liu Xue-Ying, Ma Wen-Jun, Zhang Hui-Min, Song Lei, Cai Jun, Liu Ya-Xin, Zhou Xian-Lia |
A Novel SCNN1A Variation in a Patient with Autosomal-recessive Pseudohypoaldosteronism Type 1. Journal of clinical research in pediatric endocrinology 2021 4 14 (2): 244-250. Huneif Mohammed Ayed, Alhazmy Ziyad Hamad, Shoomi Anas M., Alghofely Mohammed A., Heena Humariya, Mushiba Aziza M., AlSaheel Abdulham |
A mild and transient form of autosomal recessive Pseudohypoaldosteronism type 1 (PHA1) caused by a novel mutation in the SCNN1A gene. American journal of physiology. Endocrinology and metabolism 2023 5 . Alexandra Eythymiadou, Ivan Gautschi, Miguel Xavier van Bemmelen, Amalia Sertedaki, Aristeidis Giannakopoulos, George Chrousos, Laurent Schild, Dionisios Chrys |
A frameshift mutation in the SCNN1B gene in a family with Liddle syndrome: A case report and systematic review. Molecular medicine reports 2023 12 29 (2): . Yiting Lu, Xinchang Liu, Lin Sun, Di Zhang, Peng Fan, Kunqi Yang, Lin Zhang, Yaxin Liu, Xianliang Zh |
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- Page last updated:Mar 25, 2024
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